NO20005796L - New compounds of 12,13- (pyranosyl) -indolo [2,3-a] pyrrolo [3,4-c] carbazole and 12,13- (pyranosyl) -furo [3,4-c] indolo [2,3 -a] carbazole, process of their preparation and pharmaceutical compositions containing them - Google Patents

New compounds of 12,13- (pyranosyl) -indolo [2,3-a] pyrrolo [3,4-c] carbazole and 12,13- (pyranosyl) -furo [3,4-c] indolo [2,3 -a] carbazole, process of their preparation and pharmaceutical compositions containing them

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Publication number
NO20005796L
NO20005796L NO20005796A NO20005796A NO20005796L NO 20005796 L NO20005796 L NO 20005796L NO 20005796 A NO20005796 A NO 20005796A NO 20005796 A NO20005796 A NO 20005796A NO 20005796 L NO20005796 L NO 20005796L
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NO
Norway
Prior art keywords
indolo
carbazole
alkyl
nrarb
aryl
Prior art date
Application number
NO20005796A
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Norwegian (no)
Other versions
NO20005796D0 (en
Inventor
Michelle Prudhomme
Pascale Moreau
Fabrice Anizon
Christelle Marminon
Ghanem Atassi
Alain Pierre
Bruno Pfeiffer
Pierre Renard
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Adir
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
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Publication of NO20005796D0 publication Critical patent/NO20005796D0/en
Publication of NO20005796L publication Critical patent/NO20005796L/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/82—Carbazoles; Hydrogenated carbazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/23—Heterocyclic radicals containing two or more heterocyclic rings condensed among themselves or condensed with a common carbocyclic ring system, not provided for in groups C07H19/14 - C07H19/22
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biotechnology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Saccharide Compounds (AREA)

Abstract

A composition comprises 12,13-(Pyranosyl)-indolo(2,3-a)pyrrolo(3,4-c)carbazole and 12,13-(pyranosyl)-furo(3,4-c)indolo(2,3-a)carbazole derivatives (I), or their isomers, salts with acids or bases, are new A composition comprises 12,13-(Pyranosyl)-indolo(2,3-a)pyrrolo(3,4-c)carbazole and 12,13-(pyranosyl)-furo(3,4-c)indolo(2,3-a)carbazole derivatives of formula (I), or their isomers, salts with acids or bases, are new R1, R2 = U-V; U = 1-6C alkylene, optionally substituted by one or more halo or OH, and which may be unsaturated; V = H, halo, CN, NO2, N3, 1-6C alkyl, aryl, arylalkyl, OH, 1-6C alkoxy, aryloxy, aryl alkoxy, formyl, carboxy, aminocarbonyl, NRaRb, -CO-T1, -CO-NRa-T1, -NRa-CO-T1, -O-CO-T1, -CO-O-T1, -O-T2-NRaRb, -OT2-ORa, -O-T2-COORa, -NRa-T2-NRaRb, -NRa-T2-ORa, -NRa-T2-CO2Raor S(O)n-Ra; Ra, Rb = H, 1-6C alkyl, aryl, or arylalkyl, or both together with the N atom form a 5-7 membered heterocycle which may contain a second heteroatom (O or N) and may be substituted by alkyl, alkoxy, OH, amino, 1-6C alkylamino, or 1-6C dialkylamino; T1 = 1-6C alkyl, aryl, 1-6C arylalkyl, 1-6C alkylene, optionally substituted by -ORa, -NRaRb, -COORa, -CO-Ra, or -CO-NRaRb; T2 = 1-6C alkylene; n = 0 - 2; G = O or NR3; R3 = H, 1-6C alkyl, aryl, arylalkyl, cycloalkyl, cycloalkyl alkyl, -ORa, -NRaRb, -OT2-NRaRb, -NRa-T2-NRaRb, 1-6C hydroxylamino, dihydroxylamino, -CO-Ra, -NH-CO-Ra, 1-6C alkylene, optionally substituted by one or more of halogen, CN, NO2, -ORa, -NRaRb, -COORa, -CORa, hydroxylamino, dihydroxylamino, or -CO-NHRa; X = H, OH, 1-6C alkoxy, SH, or 1-6C alkylthio; Y = H, or X and Y together with the C atom form carbonyl; X1 = H, OH, 1-6C alkoxy, SH, or 1-6C alkylthio; Y1 = H or X1 and Y1 together with the C atom form carbonyl; R4, R5 = H, halogen, OH, alkoxy, aryloxy, aryl alkoxy, alkyl, arylalkyl, aryl, amino (optionally substituted by one or two alkyl, alkyl, aryl and arylalkyl groups), azido, -N=NRa, or -O-CO-Rc; Rc = 1-6C alkyl (optionally substituted by one or more halogen, OH, amino, alkylamino and dialkylamino groups), aryl, aralkyl, cycloalkyl or heterocycloalkyl; R6 = -U1-R4; U1 = a bond or methylene; or R4, R5, and R6 taken in pairs together with the C atoms may = 3-6 membered ring containing 1 or 2 O atoms, except for the following specific compounds: 1,11-dichloro-12,13-(1,2-(4-(O-methyl- beta -D-mannopyranosyl))-6,7,12,13-tetrahydro(5H)indolo(2,3-a)pyrrolo(3,4-c )carbazole-5,7-dio ne; 12,13-(1,2-(4-(O-methyl- beta -D-mannopyranosyl))-6,7,12,13-tetrahydro(5H)indolo(2,3-a)pyrrolo(3,4-c )carbazole-5,7-dione; 12,13-(1,2-(4-(O-methyl- beta -D-mannopyranosyl))-6,7,12,13-tetrahydro(5H)indolo(2,3-a)pyrrolo(3,4-c )carbazole-5-one; and 12,13-(1,2-(4-(O-methyl- beta -D-mannopyranosyl))-5,6,12,13-tetrahydro(7H)indolo(2,3-a)pyrrolo(3,4-c )carbazole-7-one.
NO20005796A 1999-11-17 2000-11-16 New compounds of 12,13- (pyranosyl) -indolo [2,3-a] pyrrolo [3,4-c] carbazole and 12,13- (pyranosyl) -furo [3,4-c] indolo [2,3 -a] carbazole, process of their preparation and pharmaceutical compositions containing them NO20005796L (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9914433A FR2801054B1 (en) 1999-11-17 1999-11-17 NOVEL DERIVATIVES OF 12,13- (PYRANOSYL) -INDOLO [2,3-A] PYRROLO [3,4-C] CARBAZOLE AND 12,13- (PYRANOSYL) -FURO [3,4-C] INDOLO [2,3 -A] CARBAZOLE, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Publications (2)

Publication Number Publication Date
NO20005796D0 NO20005796D0 (en) 2000-11-16
NO20005796L true NO20005796L (en) 2001-05-18

Family

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Family Applications (1)

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NO20005796A NO20005796L (en) 1999-11-17 2000-11-16 New compounds of 12,13- (pyranosyl) -indolo [2,3-a] pyrrolo [3,4-c] carbazole and 12,13- (pyranosyl) -furo [3,4-c] indolo [2,3 -a] carbazole, process of their preparation and pharmaceutical compositions containing them

Country Status (22)

Country Link
US (1) US6569858B2 (en)
EP (1) EP1101770B1 (en)
JP (1) JP3602050B2 (en)
KR (1) KR100453980B1 (en)
CN (1) CN1152040C (en)
AT (1) ATE237625T1 (en)
AU (1) AU771584B2 (en)
BR (1) BR0005426A (en)
CA (1) CA2325779C (en)
DE (1) DE60002142T2 (en)
DK (1) DK1101770T3 (en)
EA (1) EA004737B1 (en)
ES (1) ES2197061T3 (en)
FR (1) FR2801054B1 (en)
HU (1) HUP0004574A3 (en)
MX (1) MXPA00010899A (en)
NO (1) NO20005796L (en)
NZ (1) NZ508231A (en)
PL (1) PL343879A1 (en)
PT (1) PT1101770E (en)
SI (1) SI1101770T1 (en)
ZA (1) ZA200006729B (en)

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US6677450B2 (en) 2000-10-06 2004-01-13 Bristol-Myers Squibb Company Topoisomerase inhibitors
US6653290B2 (en) 2000-10-06 2003-11-25 Bristol-Myers Squibb Company Tumor proliferation inhibitors
US6610727B2 (en) 2000-10-06 2003-08-26 Bristol-Myers Squibb Company Anhydro sugar derivatives of indolocarbazoles
RU2003131269A (en) 2001-03-22 2005-05-10 Бристол-Маерс Сквибб Компани (Us) Derivatives of indolopyrrolocarbazoles and sugars, cytotoxic and selective in relation to topoisomerase I
FR2826653B1 (en) 2001-06-29 2005-10-14 Servier Lab NOVEL PYRIDO-PYRIDO-PYRROLO [3,2-G] PYRROLO [3,4-E] -INDOLE AND PYRIDO-PYRROLO [2,3-A] PYRROLO [3,4-C] CARBAZOLE DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
FR2831169B1 (en) * 2001-10-22 2003-12-12 Servier Lab NOVEL INDOLOCARBAZOLE HYDROXYALKYL DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
ES2326459B1 (en) * 2008-04-08 2010-05-28 Universidad De Oviedo GLYCOLSILATED INDOLOCARBAZOLS, ITS PROCESSING PROCEDURE AND ITS USES.
CN104031052B (en) * 2014-05-20 2016-06-08 中国科学院南海海洋研究所 Antibiotic Indimicins A E and preparation method thereof and the application in preparing antitumor drug
US10513515B2 (en) 2017-08-25 2019-12-24 Biotheryx, Inc. Ether compounds and uses thereof
CA3106239A1 (en) 2018-07-27 2020-01-30 Biotheryx, Inc. Bifunctional compounds as cdk modulators
RU2726801C1 (en) * 2019-10-16 2020-07-15 Федеральное государственное бюджетное учреждение "Национальный медицинский исследовательский центр онкологии имени Н.Н. Блохина" Министерства здравоохранения Российской Федерации (ФГБУ "НМИЦ онкологии им. Н.Н. Блохина" Минздрава России) Tumour therapy agent
WO2021222150A2 (en) 2020-04-28 2021-11-04 Anwita Biosciences, Inc. Interleukin-2 polypeptides and fusion proteins thereof, and their pharmaceutical compositions and therapeutic applications

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US5015578A (en) * 1989-03-23 1991-05-14 Bristol-Myers Squibb Company BMY-41950 antitumor antibiotic
JPH05140168A (en) * 1991-11-13 1993-06-08 Asahi Chem Ind Co Ltd Indolocarbazole derivative and antitumor agent comprising the same as active ingredient
NZ245203A (en) * 1991-11-29 1997-07-27 Banyu Pharma Co Ltd 5h-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6h)-dione derivatives substituted in position-13 by a pentose or hexose group; corresponding indolo-furano(anhydride)intermediates
JPH07112987A (en) * 1993-10-14 1995-05-02 Asahi Chem Ind Co Ltd Staurosporine sugar partial conversion derivative
CO4940430A1 (en) * 1997-07-07 2000-07-24 Novartis Ag POLYCLIC COMPOUNDS CONTAINING HYDROGENATED STAUROSPORIN WITH CONVENIENT PHARMACOLOGICAL PROPERTIES AND AN INHIBITING EFFECT ON THE GROWTH OF TUMOR CELLS

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US6569858B2 (en) 2003-05-27
EP1101770B1 (en) 2003-04-16
HK1036991A1 (en) 2002-01-25
DE60002142D1 (en) 2003-05-22
ATE237625T1 (en) 2003-05-15
EA004737B1 (en) 2004-08-26
DE60002142T2 (en) 2004-03-18
AU7168100A (en) 2002-01-03
HUP0004574A2 (en) 2001-10-28
FR2801054B1 (en) 2003-06-13
AU771584B2 (en) 2004-03-25
SI1101770T1 (en) 2003-08-31
EP1101770A1 (en) 2001-05-23
PL343879A1 (en) 2001-05-21
CN1152040C (en) 2004-06-02
DK1101770T3 (en) 2003-08-04
BR0005426A (en) 2001-07-03
EA200001078A1 (en) 2001-06-25
CA2325779C (en) 2006-07-11
HU0004574D0 (en) 2001-02-28
CA2325779A1 (en) 2001-05-17
ZA200006729B (en) 2001-06-05
FR2801054A1 (en) 2001-05-18
NO20005796D0 (en) 2000-11-16
NZ508231A (en) 2001-09-28
ES2197061T3 (en) 2004-01-01
JP2001139578A (en) 2001-05-22
JP3602050B2 (en) 2004-12-15
KR100453980B1 (en) 2004-10-20
HUP0004574A3 (en) 2001-12-28
US20020055510A1 (en) 2002-05-09
MXPA00010899A (en) 2002-05-23
KR20010051775A (en) 2001-06-25
CN1303859A (en) 2001-07-18
PT1101770E (en) 2003-07-31

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